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临床试验/NCT06389617
NCT06389617尚未招募不适用

Different Doses of Intravenous Administered Dexamethasone Effecting Brachial Plexus Supraclavicular Block for Creation of Arteriovenous Fistula in End Stage Renal Disease: A Randomized Controlled Trial

Hospital Universiti Sains Malaysia0 个研究点目标入组 50 人开始时间: 2024年5月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
50
主要终点
To compare the difference of onset time between sensory and motor block of supraclavicular block between ropivacaine with IV dexamethasone 4mg and ropivacaine with IV dexamethasone 8mg

研究概览

简要总结

To compare the analgesic properties of ultrasound guided supraclavicular block using ropivacaine 0.5% in arteriovenous fistula creation when used in combination with intravenous administered dexamethasone at 4mg and 8 mg as an adjuvant

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Supportive Care
盲法
Double (Participant, Care Provider)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult, age 18 to 65 years End stage renal disease patients for AV fistula creation

排除标准

  • Not suitable candidate as determined by the primary team Refusal for brachial plexus block History of allergy to dexamethasone or local anesthesia Pregnancy History of previous brachial plexus injury Coagulopathy Local skin site infection Known neuropathy involving the arm undergoing surgery Patients with glucose reading more then 12mmol/

研究组 & 干预措施

GROUP DF

Active Comparator

supraclavicular block with 20mls of Ropivacaine 0.5% and Intravenous dexamethasone 4mg

干预措施: supraclavicular block with 20mls of Ropivacaine 0.5% and Intravenous administered dexamethasone (Drug)

GROUP DE

Active Comparator

supraclavicular block with 20mls of Ropivacaine 0.5% and Intravenous dexamethasone 8mg

干预措施: supraclavicular block with 20mls of Ropivacaine 0.5% and Intravenous administered dexamethasone (Drug)

结局指标

主要结局

To compare the difference of onset time between sensory and motor block of supraclavicular block between ropivacaine with IV dexamethasone 4mg and ropivacaine with IV dexamethasone 8mg

时间窗: 2 days

To compare the difference in duration of analgesia between supraclavicular block with ropivacaine and IV dexamethasone 4mg with ropivacaine and IV dexamethasone 8mg

时间窗: 2 days

次要结局

  • To compare the duration difference of the return of motor block between supraclavicular block using ropivacaine with IV dexamethasone 4mg and ropivacaine with IV dexamethasone 8mg(2 days)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Prem Anand A/L Tb Nantha Kumar

Dr

Hospital Universiti Sains Malaysia

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